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NCT06441617NARecruiting

Confirmatory Trial for Alleviating Fatigue in Multiple Sclerosis

Accelerated Cure Project for Multiple Sclerosis

Start Date

12/5/2024

Completion Date

9/14/2027

Summary

CAFE-MS will assess the effectiveness of two online programs for fatigue in multiple sclerosis (MS). Although they differ, both of these online programs contain information about MS and fatigue intended to help people with MS understand and manage their fatigue. This large-scale, decentralized clinical trial is projected to enroll 2,000 people with MS. The collaboration between iConquerMS and 5 Veterans Affairs (VA) sites in the MS Centers of Excellence is designed to ensure sufficient representation of people with MS from populations traditionally under-represented in MS clinical trials. The study is a 3-arm, randomized controlled clinical trial with study participation lasting 1 year. Two of the trial arms will include one of two online programs for managing fatigue in MS added to the trial participants' usual MS treatment, and the third arm will include usual MS treatment alone. The online program phase of the trial lasts for 6 months after randomization followed by a final study visit at 12 months. Participants in the usual MS treatment alone arm for the first 6 months will have an opportunity to choose one of the online programs for the final 6 months of the trial.

Eligibility Criteria

Age Range: 22 years to No maximum

Inclusion Criteria: * Informed consent by person with MS * Living in the US * Age ≥ 22 * Confirmed diagnosis of MS by a physician, who is a neurologist or has access to a neurologist's statement of diagnosis * Fatigue Severity Scale score at or above eligibility threshold * Fluent in English * Willingness to engage in self-administration of an online intervention for 24 weeks and complete follow-up assessments * Access to the internet and e-mail with a compatible device (smartphone, computer, or tablet) * No MS relapse / no steroid treatment in the 4 weeks prior to answering the screening questionnaire (self-reported) * No disease-modifying therapeutic (DMT) started in the 4 weeks prior to answering the screening questionnaire (self-reported) Exclusion Criteria: * Unwilling or unable to consent * Refusal to saving, processing and forwarding of pseudonymized data * Concurrent participation in another interventional trial

Interventions

DEVICE

Online Program for Fatigue

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Conditions

Multiple SclerosisFatigue

Locations

Washington VA Medical Center

Washington D.C., District of Columbia 20422

United States

Baltimore VA Medical Center

Baltimore, Maryland 21201

United States

iConquerMS

Waltham, Massachusetts 02451

United States

Portland VA Medical Center

Portland, Oregon 97239

United States

Nashville VA Medical Center

Nashville, Tennessee 37212

United States

Seattle VA Medical Center

Seattle, Washington 98108

United States